EP3247437A1

EP3247437A1 - Respirator having improved synchronicity during the transition from expiratory to inspiratory operation

Info

Publication number: EP3247437A1
Application number: EP17716248.4A
Authority: EP
Inventors: Johannes Björn Thomas MEYER
Original assignee: Hamilton Medical AG
Current assignee: Hamilton Medical AG
Priority date: 2016-04-15
Filing date: 2017-04-10
Publication date: 2017-11-29
Anticipated expiration: 2037-04-10
Also published as: CN109069780A; AU2017251164A1; US20200215283A9; WO2017178440A1; DE102016206442A1; US20190134331A1; JP2019511301A; EP3247437B1

Abstract

The invention relates to a respirator (10) for the at least supportive respiration of living beings (12), wherein the respirator comprises the following: a connection formation for connection to a breathing gas supply; a breathing gas conduit arrangement (30); a pressure change arrangement (16) for changing the pressure in the breathing gas conduit arrangement (30); a flow sensor (44), which provides a flow signal (50) representing a breathing gas volume flow in the breathing gas conduit arrangement (30), a control unit (18) controlling the operation of the respirator (10). Said control unit is designed to trigger a transition from an expiratory to an inspiratory operation of the respirator (10), whenever an increase in the steepness of a flow signal curve (50) exceeds a steepness change threshold value (58). According to the invention, the control unit (18) is configured to detect the steepness change threshold value (58) depending on an expiratory time constant of the respective patient (12) to be ventilated, and to trigger the transition from an expiratory to an inspiratory operation of the respirator (10), whenever the increase in the steepness of the flow signal curve (50) exceeds the steepness change threshold value (58) determined in accordance with the expiratory time constant.

Description

Ventilator with improved synchrony in the transition from exspiratory to inspiratory operation

description

The present invention relates to a ventilator for at least assisting respiration of healthy animals breathing in the healthy state, wherein the ventilator comprises:

a connection formation for connection to a breathing gas supply,

inspiratory inspiratory respiratory gas fresh inspiratory breathing gas from the junction formation to a patient interface and metabolized in expiratory mode. expiratory breathing gas away from the patient interface leading respiratory gas conduit,

a pressure variation arrangement for varying the pressure of breathing gas in the breathing gas conduit,

a flow sensor configured and arranged to provide a flow signal representative of a flow of breathing gas at least from expiratory breathing gas in the breathing gas conduit;

a controller controlling the operation of the ventilator configured to trigger a transition from expiratory to inspiratory operation of the ventilator when an increase in the slope of a flow waveform representing successive flow signals exceeds a slope change threshold.

Such a generic ventilator is known from EP 0 521 314 A1. This document teaches switching a respirator between an expiratory phase and an inspiratory phase when the respiratory flow curve determined during the ventilation phase shows a significant increase in its steepness. Whether or not there is such a significant increase is determined based on a comparison of an increase in steepness with a predetermined slope change threshold. This lesson represents an improvement Another trigger criterion is the basic level crossing, such as a zero crossing or a passage through a non-zero base level, the respiratory flow curve, ie the temporal flow waveform , This trigger criterion is known for example from US 3,834,382. The disadvantage of this criterion is that it essentially works satisfactorily only in patients with a healthy respiratory system, whereas during the artificial respiration of chronic obstructive patients (COPD patients) unpleasant asynchronous can occur for the patient when the patient during spontaneous breathing spontaneous breathing shows. In addition, the trigger criterion of a base level crossing of the flow signal is sensitive to leakage-related effects that may occur in artificial respiration, for example because a respiratory mask, as a potential patient interface, does not completely terminate with the nose and mouth of the patient being ventilated. Other causes can cause leakage currents and thus leakage-induced effects during artificial respiration.

To avoid leakage-related errors in ETS-based triggering, DE 44 32 219 C1 teaches to increase a breathing gas flow trigger threshold for a transition from expiratory to inspiratory operation by an additional amount that is formed by the ratio between the averaged respiratory pressure during the Inspiration and the sum of the averaged breath pressures during inspiration and expiration, multiplied by the difference in the averaged values of the respiratory flows during inspiration and during expiration.

However, the known from DE 44 32 219 C1 ETS-based technical teaching can lead to patients with pathological respiratory organs, such as COPD patients, to unwanted asynchronisms during artificial respiration. From US Pat. No. 6,439,229 B1, it is also known to change ETS-based decision thresholds as a function of the expiratory time constant of the ventilated patient for a so-called "cycling", ie for a transition from inspiratory to expiratory operation of the ventilator.

ETS is termed the "Expiratory Trigger Sensitivity", which is a percentage of the maximum respiratory gas flow occurring during an inspiratory procedure that serves as the cycling threshold, when the inspiratory gas flow has dropped to the predetermined cycling threshold during the inspiratory phase In the case of healthy patients, the ETS-based cycling threshold is often about 25% of the maximum respiratory gas flow during the inspiratory phase.

US Pat. No. 6,439,229 B1 now teaches to preselect a range of possible cycling threshold values depending on the determined expiratory time constant of the respective ventilated patient and depending on the magnitude of a pressure overshoot referred to as "supra-plateau-pressure" in the respiratory gas pressure curve at the end of the pressure-assisted inspiration phase Within the preselected percentage range, select a concrete percentage of the maximum inspiratory breathing gas flow as the cycling threshold.

Although the technical teaching known from US Pat. No. 6,439,229 B1 makes it possible to improve the synchronicity of the artificial respiration by a respirator with a spontaneously breathing patient, because of the ETS-based control behavior of the known respirator it is susceptible to frequently occurring leakage currents. which can negate the synchrony advantage by the cycling threshold adjusted by the expiratory time constant and the described pressure behavior.

With the technical teaching known from the generic EP 0 521 314 A1, a comparison with ETS-based trigger and cycling threshold values is reduced. Gert susceptibility to leakage flows obtained because it no longer depends on a specific value or a concrete value ratio of the respiratory gas flow for triggering a transition from expiratory to inspiratory operation, but on the shape of the temporal breathing gas flow waveform. This shape is retained even if leakage occurs within certain limits. Also, a ventilator operating according to the teachings of EP 0 521 314 A1 can ventilate chronically obstructive patients with improved synchronicity compared to other ventilators operating approximately ETS-based ventilators. However, COPD is just one possible pathological respiratory system change. Patients with other equally occurring respiratory system changes, which lead to a deviating from a healthy breathing behavior breathing behavior can be ventilated with the known from EP 0 521 314 A1 technical teaching even with deteriorated synchrony, compared with ETS-based ventilators working.

Moreover, if both patients with undisturbed respiratory system and COPD patients are to be ventilated by one and the same ventilator operating according to EP 0 521 314 A1, the predetermined slope change threshold used in this case is always a compromise that is common to all patients should be applicable and therefore may lead in individual cases to asynchronities in the ventilation because the patient to be respirated in each case only partially applies to the case underlying the predetermined slope change threshold.

It is therefore an object of the present invention to improve the above-mentioned respirator to the effect that with him patients irrespective of the pathological state of their respiratory system with improved synchrony can be ventilated.

This object is achieved by the present invention by a generic respirator, in which the control device is further configured to determine the slope change threshold value as a function of an expiratory time constant of the respective patient to be ventilated and the transition from expiratory operation to inspiratory operation of the patient Ventilator then to trig when the increase in the slope of the flux waveform exceeds the slope change threshold determined according to the expiratory time constant. By determining, possibly changing and thus adapting the slope change threshold value depending on the expiratory time constant of each patient to be ventilated, the transition from expiratory operation to inspiratory operation of the ventilator to the pathological state of the respiratory system of the respective patient can be adjusted almost optimally, as the expiratory time constant of a person represents a highly relevant for the artificial respiration of a patient parameters.

By changing the slope change threshold value depending on the expiratory time constant of the respective patient to be ventilated, an adaptation of the operation of the ventilator at least during the transition from expiratory to inspiratory operation to any pathological conditions of the respiratory systems of patients.

It is to be understood that the term "triggering" in the present application refers only to the initiation of a transition from expiratory to inspiratory operation of the ventilator, but to trigger a transition in the opposite direction from inspiratory to expiratory, the term "cycling "used. With the control device designed according to the invention not only COPD patients, which have an above-average expiratory time constant compared to patients with healthy respiratory systems, can be ventilated with excellent synchrony, but also ARDS patients, whose expiratory time constant compared to patients with healthy respiratory systems above average is short.

One of the frequently occurring asynchronisms in the presently discussed transition from expiratory to inspiratory operation is the so-called "auto-triggering", where the ventilator triggers an inspiratory process based on pre-determined decision criteria without the patient actually inhaling or making an effort for inspiration. It then arises the situation that the respirator, the patient who wants to actually exhale or at least is about to exhale, introduces against the breath of breathing. This can trigger severe reactions in patients despite sedation, which are also unfavorable for further artificial respiration.

COPD, which is commonly referred to as "asthma" or "smoker's lung", due to the obstructive breathing behavior leads to relatively steady breathing gas flow waveforms at which a magnitude change in their steepness is relatively easy and safe to detect, so that the already known generic respirator for COPD patients provides relatively good results. ARDS patients have a restorative respiratory system, commonly referred to as a "hard" lung, where respiration is often jerky, which during one expiratory phase can lead to one or more discontinuities in the flow of breathing gas flow in the form of kinks Amount changes in the slope of the flow signal, which can trigger a car triggers at unfavorably selected slope change threshold.

The present invention also helps to ventilate ARDS patients with the inventively improved ventilator with improved synchrony. Because of the relationship described, it is advantageous to ventilate ARDS patients whose expiratory time constant is smaller than those of patients with a healthy respiratory system with a magnitude-increasing steepness change threshold in order to control ARDS-typical discontinuities in the flow signal course during an expiratory phase through the slope. Not to detect change threshold and correctly take only a magnitude larger change in the slope of the flow waveform at the end of the expiratory phase as a trigger signal, if in fact should take place in accordance with the patient behavior, a transition from expiratory to inspiratory operation. Similarly, COPD patients whose expiratory time constant is greater than those of healthy respiratory system patients may be ventilated at a slope change threshold that is lower in magnitude than that of ARDS patients and lower than that of patients with a healthy respiratory system.

Therefore, the controller is preferably configured to reduce the magnitude of the slope change threshold as the expiratory time constant increases, and vice versa.

In order to avoid undesired erroneous triggers, the control device is preferably designed to check only those changes in the steepness of the flux waveform to the presence of exceeding the steepness change threshold value by which the slope of the flux waveform increases, that is, the flux waveform progressively increases. The slope change threshold is then preferably a slope increase threshold to apply in rising flux waveform sections, but not in descending ones.

Furthermore, it should be made clear at this point that the trigger criterion discussed in the present application is not the only trigger criterion according to which the control device can change or change the operation of the ventilation device from expiratory to inspiratory. The control device preferably has a plurality, for example more than 25, trigger criteria, each of which, in the event of its presence, causes the control device to switch the operation of the ventilation device from expiratory to inspiratory.

In principle, it can be provided according to a simple embodiment of the present invention that the control device interacts with an input device, such as a keyboard and the like, by which the input of an expiratory time constant applicable to the respective patient to be ventilated is possible. Already with the mentioned flow sensor, it is basically possible to determine the expiratory time constant of a patient to be ventilated, which is why the control device is preferably designed to determine the expiratory time constant in a respective ventilation application. The flow sensor preferably detects the respiratory gas flow as a volumetric flow. An additional or alternative detection as a mass flow is also possible.

It may be thought to determine the time constant once at the beginning of the respiratory application for the entire remaining duration of the respiratory application and to perform the ventilation application with the determined value.

Alternatively, it may be considered to repeatedly determine the expiratory time constant at predetermined time intervals during a respiratory application and to continue the respiratory application with the respectively last-determined time constant value. A particularly accurate and thus advantageously particularly synchronous ventilation of a patient can be achieved by the control device being designed to detect the expiratory time constant in a breathtaking manner.

In principle, numerous possibilities are known for automatically determining an expiratory time constant of a patient. Particularly advantageous methods for this purpose are disclosed in Josef X. Brunner et al: "Simple method to measure totally expiratory time constant based on the passive expiratory volume flow curve", in: CRITICAL CARE MEDICINE, 1995, Vol. 6, pages 1 1 17 ff., Whose contents are referred to here.

For example, the control device may be designed to calculate the expiratory time constant in accordance with the ratio between the volume exhaled during an expiratory procedure and the maximum expiratory volume flow occurring, preferably iteratively numerically, and / or according to the resistance occurring during a respiratory stroke Determine compliance. Determining the resistance and the compliance separately and calculating the expiratory time constant from multiplication is possible, but less preferred than the time constant from the ratio of exhaled volume and thereby calculated maximum expiratory flow rate. Here, there are iterative numerical calculation methods which converge to a true value after only a few iteration steps, which only differs to a negligible extent from the actual time constant for the respective ventilation case.

The term "flow waveform" is not intended to be construed to record and provide the full time course of the flux signal provided by the flow sensor It is sufficient to obtain the advantages of the present invention if the flow waveform is present for such a long period of time Also, the term "flow waveform" should not be misunderstood to the effect that a continuous course is required for determining a change in the slope of it. A sequence of chronologically successive discrete flow signal values also represents a flow signal course in the sense of the present application. For example, three flow signal values ascertained chronologically one after the other suffice to determine and evaluate a change in the steepness of this short flow signal course. Thus, between the first and second flow signal value by means of a difference quotient, a slope of the flow signal course between these two interpolation points can be determined and also between the second and third flow signal value, again by a difference quotient. The slopes thus determined, once between the first and second flow signal values and once again between the second and third flow signal values, can be compared with one another, for example by subtraction, the difference value, which represents a measure of the change in the slope or steepness of the flow signal course, with the slope. Change threshold of the flow waveform can be compared. Depending on the outcome of such a comparison with the slope change threshold, then triggering may or may not be initiated.

If in the present application of successively determined or provided flow signal values is mentioned, this means preferably, but not necessarily, determined or provided directly one after the other. Of course, further possibilities for determining the change in the steepness of a flow signal course are known. For example, the flow signal profile can be approximated at least in sections by a function, which approximation function can be derived twice over time. The second derivative of a function is known to be a measure of the change in the slope of a function or a value curve.

According to an advantageous development of the present invention, provision can be made for the purposeful change of the slope change threshold on the basis of the expiratory time constant of the patient to be ventilated, in that the ventilator has a data memory at least readable by the control device, in which a relationship between the magnitude of the slope Change threshold and the expiratory time constant or a relationship between a change value of the amount of the slope change threshold value and the expiratory time constant is stored. The relationship may also affect its sign beyond the magnitude of the slope change threshold. The relationship can be stored in the form of a tabular or graphical map. A functional relationship between the magnitude of the slope change threshold value and the expiratory time constant or a functional relationship between a change value of the slope change threshold value and the expiratory time constant is preferably stored in the data memory, depending on whether the slope change threshold absolute value is determined or only one on The change amount to be applied to the previously used steepness change threshold is to be determined, that is, whether the change in the slope change threshold value should be absolute or incremental. Both are possible in principle. The control device is then preferably designed to determine an applicable slope change threshold based on the expiratory time constant on the basis of the functional relationship. Thus, no interpolation or extrapolation of steepness change thresholds need be calculated, but it may be immediate determining the slope change threshold applicable to a time constant value, optionally using the intermediate step of determining a change increment and applying the change increment to the most recent slope change threshold.

The ventilator preferably has a data memory which can be written by the control device and in which flow signal values provided by the flow sensor can be stored in order to determine from the values a temporal flow signal course. This may be the above-mentioned data store.

Frequently, the flow signal obtained from the flow sensor is noisy and therefore suboptimal suitable for immediate evaluation. Therefore, it can further be provided that the control device is designed to smooth the flow signal provided by the flow sensor, for example by low-pass filtering or by smooth averaging. The moving averaging can take into account the last five to six flow signal values, optionally weighted. A smoothing of the temporal flux waveform is particularly advantageous if the change in the slope of the flow waveform should be made by differentiating an approximated approximately to the flow waveform approximated proximity function, since an approximation function for a smooth waveform with low error can be determined. The determination of the expiratory time constant preferably takes place on the basis of the smoothed flow signal course.

In order to avoid unwanted triggering due to steepness changes in the flow waveform in the initial phase of the expiratory operation, the control device according to an advantageous embodiment of the present invention is adapted to the transition from expiratory operation to inspiratory operation of the ventilator not before a predetermined period of time after a predetermined characteristic event, such as a start of the expiratory operation or a base level crossing of the flow signal to trigger. The base level crossing of the flow signal may be a pass through a zero level or a non-zero base level. At the beginning of the exhalation vent, an inspiratory valve of the ventilator is usually closed and an expiratory valve opened, allowing the patient to reverse the direction of the respiratory gas flow. The flux signal thereby changes the sign, that is, initially falls sharply in magnitude, and then rises sharply in magnitude with the opposite sign. Starting from the maximum respiratory gas flow then occurring, the flow signal drops again in magnitude as the expiration progresses. Therefore, as a rule, at the beginning of an expiratory phase there is a change in the steepness of the flow signal course, which, however, is not intended to trigger a transition from expiratory to inspiratory operation. This is prevented with the previously described measure.

In this case, too, it may be envisaged to determine the predetermined period of time within which no transition should be triggered as of the occurrence of the characteristic event, in accordance with the expiratory time constant, since in COPD patients the expiratory phase lasts longer than in patients with a healthy respiratory system and In ARDS patients, the expiratory phase is shorter than in patients with a healthy respiratory system.

Therefore, the predetermined period of time may be shorter in ARDS patients than in patients with a healthy respiratory system and in turn shorter than that of COPD patients. The predetermined period of time can therefore be selected, for example, proportionally to the expiratory time constant.

The ventilator according to the invention is preferably designed for artificial respiration in PSV mode (PSV = "Pressure Support Ventilation").

The present invention will be explained in more detail with reference to the accompanying drawings. FIG. 1 shows a schematic representation of an artificial one according to the invention

Ventilation of a patient-equipped ventilator, FIG. 2 a shows an exemplary time profile of a flow signal of a COPD patient,

FIG. 2b is an exemplary graphical representation of increases in the slope of the flow waveform with an applicable steepness change threshold occurring in the time-flux waveform of FIG. 2a for triggering an inspiratory process;

FIG. 3 a shows an exemplary time profile of a flow signal of an ARDS patient and FIG

FIG. 3b is an exemplary graphical representation of increases in the slope of the flux waveform with an applicable transconductance change threshold occurring in the time waveform of FIG. 3a for triggering an inspiratory process.

In FIG. 1, an embodiment of a ventilation device according to the invention is designated generally by 10. The respiratory device 10 is used in the illustrated example for the artificial respiration of a human patient 12 in PSV mode.

The respiratory device 10 has a housing 14, in which - a pressure change arrangement 16 and a control device 18 can be accommodated, which is not visible from outside because of the opaque housing material. The pressure variation assembly 16 is constructed in a manner known per se and may include a pump, a compressor, a blower, a pressure vessel, a reducing valve, and the like. Next, the respiratory device 10 in a known manner, an inspiratory valve 20 and an expiratory valve 22. The control device 18 is usually realized as a computer or microprocessor. It comprises a memory device, not shown in FIG. 1, in order to be able to store and, if necessary, call up data necessary for the operation of the respiration device 10. The storage device may be in network operation Also located outside of the housing 14 and be connected by a data transmission connection to the controller 18. The data transmission connection may be formed by a cable or a radio link. However, in order to prevent malfunctions of the data transmission connection from affecting the operation of the respiratory device 10, the memory device is preferably integrated in the control device 18 or at least accommodated in the same housing 14 as the latter.

For inputting data into the respiration device 10 or, more precisely, into the control device 18, the respiration device 10 can have a data input 24, which is represented by a keyboard in the example shown in FIG. As will be explained below, the keypad is not the only data input to the controller 18. In fact, the controller 18 may receive data through various data inputs, such as via a network line, a radio link, or via sensor ports 26, discussed in greater detail below ,

To output data to the treating therapist, the respiratory device 10 can have an output device 28, in the example illustrated a screen.

For artificial respiration, the patient 12 is connected to the respiratory device 10, more precisely to the pressure change arrangement 16 in the housing 14, via a breathing gas line arrangement 30. The patient 12 is intubated for this purpose. The tube 31 forms a patient interface of the ventilator 10. Alternatively, the patient interface may include a mask covering the nose and mouth.

The respirator 10 also has a connection formation (not shown in FIG. 1) for connection to a breathing gas supply. In a simple case, this connection formation can be an intake pipe, through which ambient air - if desired with the interposition of a filter - can be sucked into the breathing gas line arrangement 30 from the immediate surroundings of the ventilator 10. The connection formation can also be a Strömungsleitungkupp- ment, by means of which the ventilator with a gas supply - be it air or oxygen - connectable. The gas supply can be, for example, a gas container or a collective supply, as it is installed in clinics as part of the building services.

The breathing gas line arrangement 30 has an inspiratory tube 32, via which fresh breathing gas can be conducted from the pressure change arrangement 16 into the lungs of the patient 12. The inspiration tube 32 can be interrupted and have a first inspiration tube 34 and a second inspiration tube 36, between which a conditioning device 38 for targeted humidification and possibly also temperature control of the patient 12 supplied fresh breathing gas can be provided. The conditioning device 38 can be connected to an external fluid reservoir 40, via which water for humidification or else a medicament, for example for inhibiting inflammation or for widening the respiratory tract, can be supplied to the conditioning device 38. When using the present ventilation device 10 as an anesthetic ventilator, volatile anesthetics can be delivered in a controlled manner to the patient 12 via the ventilation device 10. The conditioning device 38 ensures that the fresh breathing gas is supplied to the patient 12 with a predetermined moisture content, optionally with the addition of a medicament aerosol and at a predetermined temperature.

In addition to the already mentioned inspiratory valve 20 and expiratory valve 22, the breathing gas line arrangement 30 also has an expiratory tube 42, via which the metabolite is evacuated. Breathing gas is blown out of the lungs of the patient 12 into the atmosphere.

The inspiratory tube 32 is coupled to the inspiration valve 20, the expiratory tube 42 to the expiratory valve 22. Only one of the two valves is opened at the same time for the passage of a gas flow. The actuation control of the valves 20 and 22 is likewise effected by the control device 18. During a ventilation cycle, the exhalation valve 22 is initially closed for the duration of the inspiration phase, and the inspiration valve 20 is opened, so that fresh breathing gas can be conducted from the housing 14 to the patient 12. A flow of the fresh respiratory gas is effected by targeted pressure increase of the respiratory gas by the pressure change arrangement 16. Due to the increase in pressure, the fresh respiratory gas flows into the lungs of the patient 12 and expands there the body area near the lungs, ie in particular the thorax, against the individual elasticity of the body parts close to the lungs. As a result, the gas pressure inside the lung of the patient 12 also increases.

At the end of the inspiration phase, the inspiration valve 20 is closed and the expiratory valve 22 is opened. It begins the expiratory phase. Due to the increased gas pressure of the respiratory gas located in the lungs of the patient 12 until the end of the inspiration phase, this gas flows into the atmosphere after the expiratory valve 22 has been opened, the gas pressure in the lungs of the patient 12 decreasing as the flow duration progresses. If, for example, the gas pressure in the lungs 12 reaches a positive end-expiratory pressure, ie a slightly higher pressure than the atmospheric pressure, set on the respiration device 10, the expiratory phase is terminated when the expiration valve 22 closes and another ventilation cycle follows. This can be one of several trigger criteria, by the presence of which the control device can trigger a reversal of the ventilator from expiratory to inspiratory operation. During the inspiration phase, the patient 12 is supplied with the so-called respiratory tidal volume, ie the respiratory gas volume per breath. The ventilation tidal volume multiplied by the number of ventilation cycles per minute, that is, multiplied by the ventilation frequency, gives the minute volume of the present artificial respiration.

Preferably, the respiratory device 10, in particular the control device 18, is designed to repeat respiratory operating parameters that characterize the ventilation mode of the respiratory device 10 during the ventilator operation to update or to determine to ensure that the ventilator is tuned as optimally as possible to each patient to be respirated 12 at any time. The determination of one or more respiratory operating parameters with the respiration frequency is particularly advantageous, so that current and thus optimally adapted to the patient 12 ventilation operating parameters can be provided for each ventilation cycle.

The respirator 10 is communicatively coupled to at least one of a flow sensor 44, preferably further sensors, such as a pressure sensor for measuring respiratory gas pressure in the breathing gas conduit assembly 30. The flow sensor 44 detects the respiratory gas flow prevailing in the breathing gas line arrangement 30 and outputs a signal representing the respiratory gas flow or the respiratory gas flow. The flow sensor 44 is preferably coupled to the data inputs 26 of the control device 18 by means of a sensor line arrangement 46. The sensor lead 46 may or may not include electrical signal transmission lines. It can also have hose lines which transmit the gas pressure prevailing in the direction of flow on both sides of the flow sensor 44 to the data inputs 26, where these are quantified by pressure sensors (not shown in FIG. 1).

For the sake of completeness, it should be pointed out that the respiration device 10 according to the invention can be accommodated as a mobile respiration device 10 on a rollable frame 48. The flow sensor 44 is preferably located in a portion of the breathing gas conduit assembly 30 in which it can sense both the inspiratory flow and the expiratory flow. Alternatively or for redundancy reasons, in addition, at least one further flow sensor may be provided in the inspiration hose 32 and / or in the expiration hose 42 and / or in the housing 14.

FIG. 2 a shows, by way of example and roughly schematically, a temporal flow signal course 50, as is the case when the patient 12 of FIG. 1 is a COPD patient. The inspiratory process begins at time to, at which the controller 18 initiates the inspiratory process described above and increases the pressure in the inspiratory line 32 to a preset inspiratory pressure. As a result of the increase in pressure in the inspiratory tube 32, the respiratory gas flow increases rapidly, for example as a volumetric flow in volume per unit of time, and then gradually decreases in magnitude as the lung is filled with fresh respiratory gas. The respiratory gas flow toward the patient 12 or into the patient 12 is, as agreed, subject to a positive sign.

With the filling of the lungs of the patient 12 whose lungs and with this the surrounding respiratory muscles and the ribcage of the patient is stretched. At a time ti, cycling takes place, that is, a changeover of the ventilator 10 from the inspiratory mode to the expiratory mode. The inspiratory valve 20 is closed and the expiratory valve 22 is opened. As a result, the respiratory gas flow to the patient abruptly drops and reverses in its flow direction, driven by the previously increased by the introduction of fresh breathing gas into the lungs body tension in the respiratory system of the patient 12. The exhalation of the patient 12 is passive, in the to relax the parts of the body stretched by the injection of fresh respiratory gas.

As a result of the reversal of the direction of the flow of breathing gas is negative, only at time t.2 after switching the valves: inspiratory valve 20 and expiratory valve 22, the actual expiration occurs, in which the metabolized respiratory gas escapes from the lungs of the patient 12. This happens only gradually in COPD patients due to their obstructive respiratory system, so that the flow waveform 50 increases with relatively low and initially constant slope. In terms of magnitude, the flow of breathing gas decreases, but taking into account the sign of the river, it increases as it changes towards lower negative values. This means that per unit of time the metabolised breathing gas exhaled by the COPD patient decreases by an approximately constant volume flow difference. Only with advanced emptying of the lungs of the COPD patient 12 do changes, in particular increases, occur in the steepness of the flow signal course 50. For this purpose, reference is made to the three last interpolation points of the flow signal course, that is to say the interpolation points 52, 54 and 56.

As can be seen in FIG. 2 a, the magnitude of the slope or the steepness of the flow signal course 50 between the support points 52 and 54 changes in comparison to the support points which proceed in the support point 52. The slope is increasing.

The slope of the flux waveform 50 again changes between the bases 54 and 56. The slope increases again.

In FIG. 2b, the increase in the steepness is plotted over the time axis t, correlated with the time axis t of FIG. 2a. In this case, as corresponds to the representation of the flow signal course in FIG. 2a in the area of the interpolation points 52 to 56, the change in the steepness of the flux signal course 50 from the interpolation point 52 to the interpolation point 54 is plotted lower than the change in the slope of the profile compared to the previous course of the curve The changes in the steepness are respectively assigned to the temporally later interpolation points of a pair of interpolation points used for calculating the steepness, ie the interpolation points 54 and 56. The change value, in particular the increase value, the steepness of the flux waveform 50 in the region of the interpolation points 52 and 54, as compared with a preceding history section, is therefore designated 54s and the change value, in particular the increase value, of the wave signal course in the area of the support point pairs 54 and 56 relative to the section between the support point pair 50 and 52 is designated by 56s.

In addition, a slope change threshold value 58 is entered in FIG. 2b, which is used as a trigger criterion for triggering a transition from the expiratory operation to the inspiratory operation of the ventilation device 10. The slope change threshold 58 is appropriately selected in the example of FIG. 2b for COPD patients such that the change value 54s at which the patient is still in the expiratory phase and has not made his own effort for inspiration is below the slope change threshold 58 is.

However, the modifier 56s returns to a typical COPD patient value when exercising its own inspiratory effort, such that this value exceeds the transconductance threshold 58, thus causing the controller 18 to switch the ventilator 10 from an expiratory mode to an inspiratory mode.

As can be seen in FIG. 2b, a massive increase in the steepness of the flow waveform 50 occurs in the initial phase of expiration, namely at time .2, when, after the first large increase in the expiratory flow, the flow of breathing gas gradually decreases in magnitude from the patient.

In order to prevent this change in the steepness of the flow signal curve 50 from triggering a transition to inspiratory operation already at the beginning of the expiratory operation, a temporal threshold 60 is stored in the control device 18, from which only a change in the slope of the temporal flow signal curve 50 to provide a Trigger signal is observed. The temporal threshold 60 may be, for example, a predetermined period of time from the closing of the inspiratory valve 20 or from the opening of the expiratory valve 22.

FIGS. 3 a and 3 b show a representation of a flow signal course 150 corresponding to FIGS. 2 a and 2 b for an ARDS patient. ARDS patients have a so-called restruc- tive respiratory system whose compliance is very low. The respiratory system is less elastic than in respiratory healthy patients. In COPD patients, on the other hand, the resistance of the respiratory system to respiratory healthy patients is increased. Due to the decreased compliance of the respiratory system of ARDS patients, the introduction of fresh respiratory gas into the lungs of the patient requires increased work against the relatively inelastic lung and also inelastic respiratory tract. The flow waveform 150 is therefore generally steeper than in respiratory healthy patients and especially steeper than COPD patients. The maximum amounts of the river reached are also larger.

Same and functionally identical details as in FIGS. 2 a and 2 b are denoted by the same reference symbols in FIGS. 3 a and 3 b, but increased by the number 100.

As can be seen in FIG. 3a, the expiratory flow of breathing gas at the beginning of the expiratory phase reaches a value higher than in the case of a COPD patient, which is due to the obstructive breathing of the COPD patient as well as to the low compliance of the ARDS patient. For substantially the same reasons, the expiratory flow of respiratory gas in the ARDS patient falls faster in accordance with FIG. 3a than in the COPD patient.

This is also evident from the fact that the expiratory time constant of an ARDS patient has a considerably lower value than that of the COPD patient.

While in the COPD patient, the flow waveform during the expiratory phase over a long period of constant slope, the slope of the flow waveform in the ARDS patient usually changes several times during the expiratory phase.

For the evaluation of the expiratory flow waveform with regard to the presence of the change criterion of the slope of the flow waveform accounted for trigger criterion, only those changes in the slope of the flow waveform 150 are considered for the presently discussed trigger, in which the slope of the flow waveform increases 150, in which therefore the Curvature of the flow waveform 150 when viewed from the positive infinity the ordinate has a concave shape, while convex changes in steepness, at which the flux waveform 150 becomes flatter, are not considered at all. Accordingly, only those changes in the slope of the flow signal curve 150 that are positive are plotted in FIG. 3b.

It can be seen that a relatively significant increase in slope during the expiratory operation at support point 162 reaches a value which would be far beyond the slope change threshold value 58 shown in Figure 2b for COPD patients, thus triggering a transition from expiratory to inspiratory operation.

For ARDS patients, reversing the ventilator 10 in this portion of the expiratory phase would be very uncomfortable because the patient would be burdened with inspiratory flow in the middle of an expiratory procedure.

The slope change threshold 158 for ARDS patients is therefore advantageously chosen larger than that for COPD patients. A corresponding slope change threshold for respiratory healthy patients could be between thresholds 58 and 158.

At the end of the exhalation process, starting from the base 154, the PSV mode assistantly ventilated ARDS patient begins to aspirate breathing gas, which leads to a considerable increase in the steepness of the flow waveform 150. The course section between the support points 154 and 156 is significantly steeper or has a significantly greater slope than the immediately preceding course section between the support points 152 and 154. Due to the own inspiratory effort of at least occasionally spontaneously respiring during respiration ARDS patient finds this increase in the flow waveform right down to a positive flow signal. The associated change value 156s is shown in FIG. 3b. He exceeds the limit for ARDS Patients defined slope change threshold 158 and thus triggers a changeover from expiratory to inspiratory operation of the ventilator 10. A data memory of the ventilator 10 may include, in the form of a map, a table, a stored function or approximation function, and the like, a relationship between the slope change threshold to be applied in a ventilator case and an expiratory time constant characterizing the condition of the patient 12's respiratory system.

Based on the expiratory time constant of the patient 12 currently to be ventilated, the control device 18 can then use the stored relationship to query the steepness change threshold value to be used for the patient 12 currently to be ventilated or to determine it by arithmetic operations.

The expiratory time constant of the patient 12 currently being ventilated may be manually entered by medical personnel into the ventilator 10, if known, such as to have at least an initial value for the slope change threshold.

In an advantageous manner, the control device 18 is designed to determine the expiratory time constant of the respective patient 12 to be ventilated on the basis of the sensor information that is accessible to it. For this purpose, several measures are known in the art. One possible way of determining the expiratory time constant can be performed solely on the basis of the information received from the flow sensor 44. For example, the expiratory time constant can be determined on the basis of the respiratory gas volume exhaled during an expiratory phase and the maximum respiratory gas flow that has occurred during the same expiratory phase. Further possible investigation methods for determining the expiratory time constant have already been mentioned above in the introduction to the description. With the present ventilator 10 according to the invention, even patients with diametrically different pathological breathing systems with high synchronicity can thus be gently and reliably ventilated, since the ventilator 10 is able to determine the condition of the respiratory system of the patient 12 and based on the determined state of the respiratory system adapt the slope-dependent trigger criterion for a changeover of the ventilator 10 from expiratory to inspiratory operation to the respective patient to be ventilated.

Claims

claims

Respirator (10) for at least assisting ventilation of living beings (12) breathing in the healthy state, the ventilator comprising:

a connection formation for connection to a respiratory gas supply, a inspiratory breathing of fresh inspiratory breathing gas from the connection formation to a patient interface (31) leading to expiratory operation and exhaled expiratory breathing gas away from the patient interface (31) leading away from the patient interface (31) during inspiratory operation of the ventilator (10) Line arrangement (30),

a pressure variation arrangement (16) for varying the pressure of breathing gas in the breathing gas conduit arrangement (30),

a flow sensor (44) adapted and arranged to provide a flow signal (50; 150) representing a breathing gas volume flow of at least expiratory breathing gas in the breathing gas conduit (30);

a control device (18) controlling operation of the ventilator (10) and configured to trigger a transition from expiratory to inspiratory operation of the ventilator (10) when there is an increase in the slope of a flow waveform (50; 150) represents a transient change threshold (58; 158), characterized in that the control means (18) is further adapted to apply the transconductance change threshold (58; 158) depending on an expiratory time constant of the patient being ventilated (12) and trigger the transition from expiratory to inspiratory operation of the respirator (10) when the slope of the flux waveform (50; 150) increases the slope change threshold (58; 158) determined according to the expiratory time constant. exceeds. The ventilator (10) according to claim 1,

characterized in that the control means (18) is arranged to reduce the magnitude of the slope change threshold (58; 158) as the expiratory time constant increases, and vice versa.

A ventilator (10) according to claim 1 or 2,

characterized in that the control device (18) is designed to determine the expiratory time constant in a respective ventilation application.

The ventilator (10) according to claim 3,

characterized in that the control device (18) is designed to detect the expiratory time constant breathtaking.

A ventilator (10) according to claim 3 or 4,

characterized in that the control device (18) is adapted to the expiratory time constant in accordance with the ratio of exhaled volume and in this expiratory event occurred maximum expiratory volume flow, preferably iteratively numerically, and / or in accordance with the occurring during a breath resistance and compliance determine.

A ventilator (10) according to any one of the preceding claims,

characterized in that it comprises a data memory at least readable by the control device (18), in which a relationship between the amount of the steepness change threshold (58; 158) and the expiratory time constant or a relationship between a change value of the amount of the slope change threshold ( 58, 158) and the expiratory time constant.

The ventilator (10) according to claim 6,

characterized in that in the data memory a functional relationship between the magnitude of the slope change threshold (58; 158) and the expiratory time constant or a functional relationship between a change value of the magnitude of the slope change threshold (58; 158) and the expiratory time constant and that the control means (18) is adapted to apply a slope change threshold (58; 158 ) on the basis of the expiratory time constant on the basis of the functional relationship.

A ventilator (10) according to any one of the preceding claims,

characterized in that the control device (18) is designed to smooth the flow signal (50; 150) provided by the flow sensor (44), for example by low-pass filtering or by sliding averaging.

A ventilator (10) according to any one of the preceding claims,

characterized in that the control means (18) is adapted to prevent the transition from expiratory operation to inspiratory operation of the ventilator (10) not before a predetermined period of time (60; 160) has elapsed after a predetermined characteristic event, such as commencement of expiratory operation or triggering a base level crossing of the flow signal (50; 150).

0. respirator (10) according to claim 9,

characterized in that the controller is adapted to determine the predetermined period of time (60; 160) in accordance with the expiratory time constant.